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About the Company
Technology-led healthcare and consulting organization working with global life sciences clients, delivering digital, regulatory and pharmacovigilance solutions across international markets.
Role & Responsibilities
• Act as Subject Matter Expert for Drug Safety and Pharmacovigilance
• Track evolving global regulatory and compliance requirements
• Partner with sales and solutioning teams to improve win ratios
• Provide strategic inputs for RFP and RFI responses
• Build and enhance safety service offerings and capability decks
• Design cost-effective and competitive safety value propositions
• Develop senior-level client relationships across PV and Safety
• Represent organization at industry conferences and forums
• Lead safety consulting engagements and provide operational oversight
Qualification
• MBBS (mandatory)
Eligibility
• 15+ years total experience
• 8–10+ years in Drug Safety / Pharmacovigilance
• Career must have started in corporate pharma, CRO or life sciences organization
• Strong regulatory knowledge (FDA and global)
• Hands-on experience with Argus, ARISg and MedDRA
• Excellent analytical, communication and stakeholder management skills
Salary
• As per industry standards
Benefits
• Strategic leadership role
• High-impact global exposure
• Opportunity to influence business growth and safety strategy
• Participation in global conferences and industry forums
• Leadership visibility and consulting exposure